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[肿瘤坏死因子α抑制剂治疗期间的神经并发症]

[Neurological complications during treatment of the tumor necrosis alpha inhibitors].

作者信息

Piusińska-Macoch Renata

机构信息

Klinika Neurologii, Centralnego Szpitala Klinicznego Ministerstwa Obrony Narodowej, Wojskowy Instytut Medyczny w Warszawie.

出版信息

Pol Merkur Lekarski. 2013 May;34(203):293-7.

Abstract

Medications with TNF-alpha inhibitors family are successfully applicable in rheumatology, gastroenterology, dermatology and neurology. Still, the ongoing research on the safety assessment of their application, also due to neurological complications. The vast majority of these complications is associated with an increased risk of serious virus (Herpes simplex--JC) and bacterial (Listeria monocytogenes) neuroinfections. They can cause the occurrence of progressive multifocal leukoencephalopathy--PML with a severe clinical course and poor prognosis or herpes simplex encephalitis--HSE. Meta-analysis revealed a number of cases of PML and the HSE in the first 6 months of treatment with natalizumab, efalizumab, rituximab, abatacept and infliximab. Common complication occasionally turning on this biologics is chronic demyelinating polyneuropathy or Lewis-Sumner syndrome. Described are cases of central and peripheral demyelination typical of multiple sclerosis (MS). Are also reported cases of motor multifocal neuropathy with conduction block acute encephalithis with polyneuropathy or mononeuropathy in the form of anterior optic neuropathy Guillen-Barre' syndrome and its variant, Miller-Fisher syndrome have been confirmed as adverse events following treatment with infliximab. Also revealed several cases of myasthenia gravis after using etanercept. In the few cases of systemic lupus CNS involvement caused by treatment with TNF inhibitors, the mechanism of these disorders is still considered too vague. Due to the emerging reports on the number of neurological adverse events of TNF antagonists, significantly higher than those described in the literature, the safety of their use requires further monitoring and multicenter studies.

摘要

肿瘤坏死因子-α抑制剂类药物已成功应用于风湿病学、胃肠病学、皮肤病学和神经病学领域。然而,由于神经并发症,对其应用安全性的研究仍在进行中。这些并发症绝大多数与严重病毒(单纯疱疹病毒-JC)和细菌(单核细胞增生李斯特菌)神经感染风险增加有关。它们可导致进展性多灶性白质脑病(PML)的发生,临床病程严重且预后不良,或导致单纯疱疹病毒性脑炎(HSE)。荟萃分析显示,在使用那他珠单抗、依法珠单抗、利妥昔单抗、阿巴西普和英夫利昔单抗治疗的前6个月内,出现了多例PML和HSE病例。使用这类生物制剂偶尔出现的常见并发症是慢性脱髓鞘性多发性神经病或Lewis-Sumner综合征。描述了多发性硬化症(MS)典型的中枢和外周脱髓鞘病例。也有报告称,英夫利昔单抗治疗后出现了伴有传导阻滞的运动性多灶性神经病、急性脑脊髓炎伴多发性神经病或单神经病,表现为前部视神经病变、吉兰-巴雷综合征及其变异型米勒-费希尔综合征等不良事件。使用依那西普后也发现了几例重症肌无力病例。在少数由肿瘤坏死因子抑制剂治疗引起的系统性狼疮中枢神经系统受累病例中,这些疾病的机制仍被认为过于模糊。由于关于肿瘤坏死因子拮抗剂神经不良事件数量的新报告显著高于文献中描述的数量,其使用安全性需要进一步监测和多中心研究。

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